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Researcher
Herman Pieterse
Profile
Projects
Publications
Activities
Awards & Distinctions
15
Results
2017
Good clinical practices in (nuclear) research
Herman Pieterse
Jan Pruim
Bookchapter
in
Quality in nuclear medicine
2017
2015
Guidance for the regulatory status of allergen extracts in clinical trials
Zuzana Diamant
Maurits van Maaren
Roy Gerth van Wijk
Jacobus RBJ Brouwers
Herman Pieterse
A1
Journal Article
in
EUROPEAN RESPIRATORY JOURNAL
2015
2014
Good clinical practice in clinical interventional studies
Herman Pieterse
Zuzana Diamant
A2
Journal Article
in
EUROPEAN CLINICAL RESPIRATORY JOURNAL
2014
2008
Regulatory-clinical methodologies for medical device clincal trials
Herman Pieterse
Lucas Van Bortel
Paul Van Cauwenberge
Dissertation
2008
2007
A vision for Eu Device Regulation.
Herman Pieterse
M DE JONG
A2
Journal Article
in
Regulatory affairs journal. Devices
2007
Essentials of Good Regulatory Compliance: the REACT principles.
Herman Pieterse
M DE JONG
Book
2007
Is the Migraid (R) device an asset in the non-pharmacologic treatment of migraine?
Herman Pieterse
JAM KUSTER
Lucas Van Bortel
A1
Journal Article
in
ACTA NEUROLOGICA BELGICA
2007
State of the art clinical trials for medical devices: a guide to Good Clinical Practices compliance.
M DE JONG
Herman Pieterse
Book
2007
The future of the EU Medical Device Regulatory System: globalisation, simplification, centralisation and automation.
M DE JONG
Herman Pieterse
Book
2007
2006
Een degelijke klinische ontwikkeling van medische hulpmiddelen is een vereiste om de continuïteit van zorg te garanderen.
Herman Pieterse
MG DE JONG
A3
Journal Article
in
NEDERLANDS TIJDSCHRIFT VOOR MEDISCHE ADMINISTRATIE
2006
Proper clinical development of medical devices to ensure continuity of care.
Herman Pieterse
M DE JONG
A3
Journal Article
in
Health Information Developments in the Netherlands
2006
The essentials of Good Regulatory Compliance.
Herman Pieterse
M DE JONG
A2
Journal Article
in
Regulatory affairs journal. Devices
2006
2005
The changing regulatory environment for the clinical evaluation of medical devices in Europe.
Herman Pieterse
M DE JONG
A2
Journal Article
in
REGULATORY AFFAIRS JOURNAL. DEVICES
2005
2004
Instruction manual for the conduct of clinical research with medicinal products in the Netherlands: a practical guide for the design, preparation, conduct and reporting.
Herman Pieterse
A COHEN
M POLS
Book
2004
Richtsnoer voor Good Clinical Practice (CPMP/ICH/135/95).
Herman Pieterse
Book
2004